FDA UDI In Commercial Distribution 🇺🇸 United States

O-ARM®

DI: 00643169868137 · Model: 9732721 · MEDTRONIC NAVIGATION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
O-ARM®
Primary DI
00643169868137
Version / Model
9732721
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
803580559
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-07
Public Version
1
Public Version Date
2024-04-15
Public Version Status
New
Public Device Record Key
db550b5a-2448-4bc2-bb7a-8491287658e7

Device Description

MOUSE 9732721 STERILE O-ARM 10

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OXO Image-intensified fluoroscopic x-ray system, mobile

GMDN Terms

Code Name
37649 Portable general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Package 20643169868131
Primary 00643169868137

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K060344 000